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Israel Freeman, MD Associate Professor of Clinical Medicine
Pericardial Diseases Israel Freeman, MD Associate Professor of Clinical Medicine
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Diseases of the Pericardium
Acute Pericarditis Pericardial Effusion Constrictive Pericarditis
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Acute Pericarditis
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Acute Pericarditis common causes
Outpatient setting usually idiopathic probably due to viral infections Coxsackie A and B (highly cardiotropic) are the most common viral cause of pericarditis and myocarditis Others viruses: mumps, varicella-zoster, influenza, Epstein-Barr, HIV
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Diseases of the Pericardium
Acute Pericarditis Primary: Usually due to viral infection Course brief and usually uncomplicated Secondary Result from other conditions: rheumatic or collagen diseases, radiotherapy or rend failure related, often exhibit clinical feature, similar to acute pericarditis
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Acute Pericarditis common causes
In-patient setting T = Trauma, TUMOR U = Uremia M = Myocardial infarction (acute, post) Medications (hydralazine, procainamide) O = Other infections (bacterial, fungal, TB) R = Rheumatoid, autoimmune disorder, Radiation
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Special Ethiologic Forms of acute Pericarditis and Pericardial Effusion
Renal failure and dialysis: more extensive dialysis and NSAID is usually successful occasionally pericardocentesis necessary unexpected drop of B.P during dialysis may be the clue Radiation induced pericardial effusion: After radiation to the mediastinum May evolve into constrictive Pericarditis after many years Neoplastic pericardial effusion Accounts for 50% of patient with tamponade Lung, Breast cancers accounts for majority of causes, lymphomas and leukemia also important causes Purulent Pericarditis: usually requires surgical draming Drug induced Pericarditis: Procainamide, Minoxidil, Methylsergide Post Cardiotomy Syndrome
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Acute Pericarditis Diagnostic Clues
History sudden onset of anterior chest pain that is pleuritic and substernal Physical exam presence of two- or three-component rub ECG most important laboratory clue
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Acute Pericarditis Differential Diagnosis
Acute myocardial infarction Pulmonary embolism Pneumonia Aortic dissection
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Acute Pericarditis Chest Pain History pericarditis vs infarction
Common characteristics retrosternl or precordial with raditaion to the neck, back, left shoulder or arm Special characteristics (pericarditis) more likely to be sharp and pleuritic with coughing, inspiration, swallowing worse by lying supine, relieved by sitting and leaning forward
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Acute Pericarditis Heart Murmurs of Pericarditis
Pericardial friction rub is pathognomic for pericarditis scratching or grating sound Classically three components: presystolic rub during atrial filling ventricular systolic rub (loudest) ventricular diastolic rub (after A2P2
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Acute Pericarditis ECG in stage 1 of pericarditis shows PR segment depression and ST elevations.
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Stages of ECG Evolution in Acute Pericarditis
PR segments ST segments T waves 1 Depressed Elevated Upright 2 Isoelectric Isoelectric Flat 3 Isoelectric Isoelectric Inverted 4 Isoelectric Isoelectric Upright
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ECG in Acute Pericarditis
EKG contrast the pattern of ST segment elevation characteristic of acute pericarditis (a) with the normal variant (early repolarization) pattern of ST segment elevation (b). The normal variant pattern is associated with a normal or slow heart rate and has relatively tall R waves and T waves in V4, V5, and V6. The ST segment elevation is less than 25% of the T wave amplitude. In contrast, the acute pericarditis has PR depression and lower T wave.
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Acute Pericarditis ECG features
ST-segment elevation reflecting epicardial inflammation leads I, II, aVL, and V3-V6 lead aVR usually shows ST depression ST concave upward ST in AMI concave downward like a “dome” PR segment depression early stage T-wave inversion occurs after the ST returns to baseline
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Pericarditis Acute apical infarction Early Repolarization
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Acute Pericarditis Management
Analgesic agents codeine mg q 4-6 hr Anti-inflmmatory agents Treat underlying cause ASA 648 mg q 3-4 hrs NSAID (indomethacin mg qid) Corticosteroids are symptomatically effective , but preferably avoided
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Acute Pericarditis Diagnosis Treatment Chest pain
Friction rub, fever, Tachycardia EKG changes are common (diffuse ST-T changes with absence of reciprocal ST depression when ST elevation is present, depressed PR segment) Mild elevation of cardiac enzymes Treatment Analgesics – codeine, hydrocodone NSAID – Indomethacin (100 mg/d) Corticosteroids – (40 – 60 mg/d) , slow tapering (2 – 4 weeks) due to possible recurrence after steroid withdrawal
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Other forms of Acute Pericarditis
Relapsing Pericarditis Acute Pericarditis of any etiology may relapse Treatment: Colchicine, Prednisone or immnosuppressants Progression to constriction Rarely acute pericarditis progresses to subucute / chromic
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Other Forms of Pericarditis Dressler’s Syndrome
Described by Dressler in 1956 fever, pericarditis, pleuritis (typically with a low grade fever and a pericardial friction rub) occurs in the first few days to several weeks following MI or heart surgery incidence of 6-25% treat with high-dose aspirin
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Other Forms of Pericarditis Bacterial Pericarditis
Rare condition in antibiotic era (steadily decreased over last 40 years) Typically arises from contiguous spread of intrathoracic infection (pneumonia, empyema, mediastinitis, endocarditis, trauma, surgery) Usually fatal without adequate treatment Diagnosis frequently missed Often lacks characteristic features of acute pericarditis
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Other Forms of Pericarditis Purulent Pericarditis (data from 15 patients)
# 3 2 mediastinitis esophageal tear, dental abscess retropharyngeal abscess, chest trauma, post-cardiac surgery infection endocarditis, prosthetic aortic valve pneumonia (with empyema) hepatic abscess (with empyema) bacterial meningitis diabetes, leukemia, bone marrow transplant 1 1 1 1 3 Arch Int Med 1996; 156:1857
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Other Forms of Pericarditis Tuberculous Pericarditis
Incidence of pericarditis in patients with pulmonary TB ranged from 1-8% Physical findings: fever, pericardial friction rub, hepatomegaly TB skin test usually positive Fluid smear for TB often negative Pericardial biopsy more definitive
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Acute Pericarditis Key Points
• Acute pericarditis is accompanied by pericardial effusion in 60% of cases and tamponade in as many as 15% of cases. • Outpatient management of acute idiopathic pericarditis is acceptable if there is no effusion at predischarge echocardiography and surveillance can be provided at home. • In the care of patients in clinically stable condition who are being hospitalized, echocardiography should be performed in the first 24 hours because a large effusion is the best predictor of poor outcome
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Pericardial Effusion and Cardiac Tamponade
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Pericardial Effusion and Cardiac Tamponade
Fluid can accumalte in the pericardium in any form of pericardial disease Transudate Exudate Serosanguineous: Idopathic, dialysis-related, neoplastic, radiation induced, TB, coagulapaties Bloody: Coagulopathies, trauma, rupture in MI and in aortic dissection Cardiac Tamponade is the most important complication of fluid accumulation
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Cardiac Tamponade pathophysiology
Fluid accumulation within the pericardial space resulting in increased intracardiac pressure progressive limitation of ventricular diastolic filling reduction of stroke volume and cardiac output
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Cardiac Tamponade The physiological effect depends on the rate of fluid accumulation Gradually the pericardium may strech and accommodate > 2,000 ml Acutely as little as 200 ml of accumulated fluid may raise the intrapercardial pressure to cause tamponade JVD elevated (rarely not in low pressure tamponade) B.P variable, paradoxical pulse (>10 mm HG ) Echocardiography Treatment: fluids, pericardiocentesis, cardiac surgery.
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Cardiac Tamponade Beck’s Triad
Described in 1935 by thoracic surgeon Claude S. Beck 3 features of acute tamponade Decline in systemic arterial pressure Elevation in systemic venous pressure (e.g. distended neck vein) A small, quiet heart
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Etiologies of Cardiac Tamponade
malignancy idiopathic pericarditis uremia acute myocardial infarction diagnostic procedures with cardiac perforation bacterial tuberculosis radiation myxedema dissecting aortic aneurysm post pericardiotomy syndrome systemic lupus erythematosus cardiomyopathy
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Cardiac Tamponade Early stage Advanced stage
mild to moderate elevation of central venous pressure Advanced stage intrapericardial pressure ventricular filling, stroke volume hypotension impaired organ perfusion
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Cardiac Tamponade Clinical Features
Symptoms dyspnea, fatigue, agitation and restlessness, syncope, shock, anuria Physical examination pulsus paradoxus tachycardia increased jugular venous pressure hypotension
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Cardiac Tamponade Pulsus Paradoxus tamponade without pulsus
atrial septal defect severe aortic stenosis aortic insufficiency left ventricular dysfunction LVH with LVEDP decreased intravascular volume (low-pressure tamponade) pulsus without tamponade COPD RV infarct pulmonary embolism effusive constrictive pericarditis restrictive cardiomyopathy extreme obesity tense ascites
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Central Venous Pressure
Cardiac Tamponade Central Venous Pressure X - descent descent of the base in systole Y - descent occurs as the tricuspid valve opens and ventricular filling begins from the high-pressure right atrium in constrictive pericarditis, filling is truncated in early to mid diastole in tamponade, filling is restricted throughout diastole Kussmaul’s Sign in constriction, venous return increases with inspiration and a high right atrial pressure resists filling resulting in an increased JVP
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Central Venous Pressure
Cardiac Tamponade Constrictive Pericarditis presence of a rapid Y-descent argues against cardiac tamponade
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Cardiac Tamponade Pulsus Paradoxus
an exaggerated drop in SBP with inspiration (>10mmHg)
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Pressure Readings in Cardiac Tamponade
The aortic pressure and right atrial pressure are recorded during quiet breathing in a patient with cardiac tamponade. The marked fall in arterial pressure that occurs during inspiration is a paradoxical pulse. The decrease in pulse pressure, defined as the difference between systolic and diastolic pressures, that accompanies the fall in systolic pressure indicates that left ventricular stroke volume decreases during inspiration. Central venous pressure, as indicated by the right atrial pressure, also falls during inspiration.
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Cardiac Tamponade Dignostic Evaluation Chest x-ray Echocardiography
usually requires > 200 ml of fluid cannot distin guish between pericardial effusion and cardiomegly Echocardiography standard for diagnosing pericardial effusion convenient, highly reliable, cost effective false positives (M-mode)- left pleural effusion, epicardial fat, tumor tissue, pericardial cysts
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ECG in Pericardial Effusion
Diffuse low voltage amount of fluid electrical conductivity of the fluid Electrical alternans alternating amplitude of the QRS produced by heart swinging motion also seen in PSVT, HTN, ischemia
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ECG: Pericardial Effusion
The electrocardiogram (V2 lead) from a patient with pericardial effusion caused by malignant melanoma reveals a low voltage and electrical alternans.
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Echocardiographic Diagnosis
Cardiac Tamponade Echocardiographic Diagnosis Pericardial effusion highly reliable Cardiac tamponade RA and RV diastolic collapse reduced chamber size distension of the inferior vena cava exaggerated respiratory variation of the mitral and tricuspid valve flow velocities
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Pericardial Effusion-Echocardiography
Pericardial effusion is seen in the two-dimensional echocardiogram as an echo-free space outside the cardiac chambers. Two characteristic sites are lateral to the left ventricle in the apical four-chamber view (shown here) and posterior to the left ventricle in the parasternal long-axis view (see Figure 3b).
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RA and RV diastolic collapse
early diatole systole late diastole
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CT Scan: Pericardial Effusion
A chest CT scan of a patient with pericardial effusion, pericardial fluid appears less dense than the heart and is separated from the myocardium by epicardial fat in some areas.
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Echocardiogram: Pericardial Effusion
The echocardiogram demonstrates that the heart moves forward (F) and backward (B) within the effusion on alternate beats, thus producing the alternation of the QRS axis characteristic of electrical alternans. The heart also moves with inspiration (Insp) and expiration (Exp), which accounts for a change in anterior wall motion with every two cardiac cycles.
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Differential Diagnosis of Cardiac Tamponade vs
Differential Diagnosis of Cardiac Tamponade vs. Chronic Constrictive Pericarditis Differences between the central venous pulse contours characteristic of cardiac tamponade (left) and chronic constrictive pericarditis (right) provide the basis for differential diagnosis. The pressure contour in a patient with pericardial effusion and tamponade has a prominent systolic dip (X) but little or no diastolic deflection. The central venous pulse pattern in a patient with chronic constrictive pericarditis displays an M or W contour consisting of both systolic dip (X) and diastolic dip (Y), the Y descent being more prominent.
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CT Scan in Chronic Constrictive Pericarditis
In this CT scan of the chest of a patient with chronic constrictive pericarditis, the dense layer on the anterior surface of the heart represents thickened and partially calcified pericardium.
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Cardiac Tamponade Treatment Options
Nonsurgical pericardiocentesis blind ECG guided Echo guided CT guided balloon pericardiotomy Surgical subxiphoid video-assisted thoracoscopy pericardial-peritoneal pericardial window pericardiectomy
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Cardiac Tamponade Pericardiocentesis Diagnostic tap
usually not indicated rarely have positive cytology or infection that can be diagnosed Therapeutic drainage indicated for significant elevation of the central venous pressure
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Cardiac Tamponade Pericardial Window
Balloon dilatation of a needle pericardiostomy subxyphoid surgical pericardiostomy video-assisted thoracoscopy with localized pericardial resection anterolateral thoracotomy with parietal pericardial resection
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Localized and Low Pressure
Cardiac Tamponade Localized and Low Pressure Localized tamponade due to loculated pericardial effusion Low pressure tamponade due to relative intravascular volume depletion
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Constrictive Pericarditis Idiopathic Restrictive Cardiomyopathy
Clinical Features That Differentiate Constrictive Pericarditis from Amyloidosis and Idiopathic Restrictive Cardiomyopathy Clinical Feature Constrictive Pericarditis Cardiac Amyloidosis Idiopathic Restrictive Cardiomyopathy Early diastolic sound (S3 or pericardial knock) Frequent Occasional Late diastolic sound (S4) Rare Atrial enlargement Mild or absent Marked Atrioventricular or intraventricular conduction defect QRS voltage Normal or low Low Normal or high Mitral or tricuspid regurgitation Paradoxical pulse Frequent but usually mild Exaggerated variation in mitral and tricuspid flow velocity with respiration, out of phase Usual
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Constrictive Pericarditis (concretio cordis)
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Constrictive Pericarditis
An uncommon post inflammatory disorder the encasement of the heart by a rigid, nonpliable pericardium characterized by a thickened, fibrotic, and frequently calcified pericardium rarely develop after an episode of acute idiopathic pericarditis more likely to develop after subacute pericarditis with effusion that evolve over several weeks
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Causes of constrictive pericarditis
idiopathic infectious tuberculosis virus bacteria histoplasmosis drugs hydralazine cromolyn sodium procainamide penicillins isoniazid minoxidil phenylbutazone methysergide radiation chest trauma or surgery epicardial defibrillator patches connective tissue disease SLE, RA, dermatomyositis renal failure (on dialysis) myocardial infarction neoplasm sarcoidosis porphyria cutanea tarda asbestosis Whipple disease
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Constrictive Pericarditis Differential Diagnosis
restrictive cardiomyopathy right ventricular failure mitral and tricuspid valve disease cardiac tamponade
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Constrictive Pericarditis Clinical Findings
Jugular venous elevation 96% prominent X- and Y-descent, “M” or “W” 94% with inspiration (Kussmaul’s sign) Heart diastolic pericardial knock % absent or decreased apical impulse Abdomen: ascites % pulsatile hepatomegaly 70% Extremities: peripheral edema Pulsus paradoxus almost always < 10 mm Hg; otherwise, considered tamponade
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Constrictive Pericarditis Diagnosis
insidious onset , often not recognized in its early phases by exam, x-ray, ECG, echo average duration of symptoms before diagnosis was 23.4 months ( range 1 to 264 months) tendency to overlook elevated JVP subacute chronic diastolic knock Kussmaul’s pulsus paradoxus < 10 mm Hg
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Constrictive Pericarditis Diagnostic Tests
Electrocardiogram sinus tachycardia, atrial fibrillation, ST flattening, T-wave inversion, low QRS voltage, right axis deviation / RVH Chest radiograph pericardial calcification (44% to 70% in the past), must be distinguished from left ventricular aneurysm calcification MR I and computed tomography pericardial thickening over the right ventricle (sensitivity 88%, specificity 100%, diagnostic accuracy 93%)
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Pericardial Calcification
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CT Scan in Chronic Constrictive Pericarditis
In this CT scan of the chest of a patient with chronic constrictive pericarditis, the dense layer on the anterior surface of the heart represents thickened and partially calcified pericardium.
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Constrictive Pericarditis Echocardiography
M-mode echo abrupt flattening of mid to late diastolic movement of the LV posterior free wall diastolic septal bounce TTE / TEE normal pericardium 1.2 0.8 mm 3 mm cut off has a sensitivity of 95% and specificity of 86%
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Constrictive Pericarditis Effect of respiration on pulsed-wave Doppler pattern
Mayo Clin Proc
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Constrictive Pericarditis Doppler vein flow velocities
pulmonary venous flow velocity peak systolic and diastolic values decrease with inspiration
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Constrictive Pericarditis
Hemodynamics End-diastolic pressures elevated and equalized (<5 mm Hg difference) RA pressure tracing rapid X- and Y-descent, “W” or “M” pattern failure to decrease with inspiration (Kussmaul’s sign) RV pressure RVEDP > 1/3 of RVSP dip and plateau configuration of RVDP (square root sign) LV and RV pressures discordant changes
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Hemodynamics of Constrictive Physiology variability in early-daistolic PCW-LV gradient with respiration
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Pericardiectomy cardiac decortication
Constrictive Pericarditis Pericardiectomy cardiac decortication In hospital mortality vary between 0% and 10% predictors of poor outcome: underlying malignancy radiation-induced previous paracardial surgery NYHA class IV symptoms myocardial atrophy myocardial inflammation and scarring
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